Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review-Reference-Cited by-同舟云学术

Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review

Published:2018-01-09 Issue:1 Volume:10 Page:
ISSN:1758-9193
Container-title:Alzheimer's Research & Therapy
language:en
Short-container-title:Alz Res Therapy

Author:

Ygland Emil,van Westen Danielle,Englund Elisabet,Rademakers Rosa,Wszolek Zbigniew K.,Nilsson Karin,Nilsson Christer,Landqvist Waldö Maria,Alafuzoff Irina,Hansson Oskar,Gustafson Lars,Puschmann Andreas

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1186/s13195-017-0330-2.pdf

Reference53 articles.

1. Kovacs GG. Invited review: neuropathology of tauopathies: principles and practice. Neuropathol Appl Neurobiol. 2015;41(1):3–23.

2. Ghetti B, Oblak AL, Boeve BF, Johnson KA, Dickerson BC, Goedert M. Invited review: frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging. Neuropathol Appl Neurobiol. 2015;41(1):24–46. A published correction appears in Neuropathol Appl Neurobiol. 2015;41(4):571.

3. Hirschbichler ST, Erro R, Batla A, Bhatia KP. Classic PD-like rest tremor associated with the tau p.R406W mutation. Parkinsonism Relat Disord. 2015;21(8):1002–4.

4. Lindquist SG, Holm IE, Schwartz M, Law I, Stokholm J, Batbayli M, et al. Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation. Eur J Neurol. 2008;15(4):377–85.

5. Rosso SM, Kamphorst W, Ravid R, van Swieten JC. Coexistent tau and amyloid pathology in hereditary frontotemporal dementia with tau mutations. Ann N Y Acad Sci. 2000;920:115–9.

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Tau filaments with the Alzheimer fold in cases withMAPTmutations V337M and R406W;2024-04-30

2. A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy;Frontiers in Neurology;2024-04-19

3. Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of MAPT Mutations: A Systematic Review;Frontiers in Bioscience-Landmark;2024-01-16

4. Systems pharmacology and multi-scale mechanism of Enicostema axillare bioactives in treating Alzheimer disease;Inflammopharmacology;2023-10-16

5. Genetics of Multiple System Atrophy and Progressive Supranuclear Palsy: A Systemized Review of the Literature;International Journal of Molecular Sciences;2023-03-09